Реакция #64980

ord-a308aae1db5a42ab888d2ce88b8252cc

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThen the catalyst is filtered off
  2. 2
    Концентрированиеthe filtrate is concentrated by evaporation

Методика

17.5 g (70 mmol) of 5-methyl-1,4-dihydropyridine-2,3dicarboxylic acid N-benzylimide are hydrogenated in 150 ml of tetrahydrofuran at 70° C. and under 100 bar over palladium on active charcoal. Then the catalyst is filtered off and the filtrate is concentrated by evaporation. The solid oily residue (13.0 g) is used as a crude product in the next stage.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05416096uspto-grants-1995_05